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Life’s Blind Illumination
If you’ve stumbled upon this little corner of the internet, thank you for being here. I’m just a guy who’s spent most of his life chasing light through a lens, and lately, that light has started to fade in ways I never quite imagined. This post isn’t meant to be a pity party or a grand manifesto, I’m no expert on resilience, just someone muddling through with a heart full of gratitude and a camera bag that’s gotten a bit lighter over the months. But writing has always been a quiet companion to my photography, a way to make sense of the frames I capture (or, these days, the ones I remember). So, with a deep breath and a humble nod to God, here’s where my story sits right now.
It started with a simple video. Yesterday, I hit record on my phone for Instagram, a raw, rambling clip from the heart about the sting of going blind and what that means for the photographs I’ve loved making. I poured out the ache of knowing I can’t nail those perfect compositions or exposures anymore, the kind that come from years of squinting at a scene with my one good eye and just knowing. Film has its own personality, doesn’t it? Fomapan with its moody shadows and tight latitude, Kentmere offering a bit more forgiveness in the highlights. Details like that live in my head, etched from decades of trial and error. But my eyes? They’ve decided to bow out early. Five doctors, the state of Arizona, and the U.S. government all agree: I’m beyond legally blind, teetering on the edge of total darkness. I wake up each morning bracing for the day it all goes black.
About two months back, the warning signs ramped up. Closing my eyes brought flashes of random colors and lights, like a faulty projector spinning out of control. That sliver of vision I had left, five degrees on a good day, turned blurry, turning the world into soft-edged blobs. I laughed it off in an article I wrote, calling everyone a “blob” because, well, humor’s been my shield against the heavy stuff. But reality doesn’t stay polite for long.
One afternoon, I picked up one of my trusty SLR film cameras, the kind that’s felt like an extension of my hand for years. I tried to focus. Couldn’t. The viewfinder swam into nonsense. Composition? Forget it—that narrow tunnel of sight wasn’t enough to frame a thought.
I found myself on a park bench that day, head in hands, weeping for what felt like hours. Self-pity wrapped around me like fog, thick and unyielding. It was the first time I’d let the full weight of it crash down. I haven’t lifted a camera to shoot since, not one single frame. In the haze of those weeks, I started selling off pieces of my collection, each transaction a quiet goodbye to the tools that shaped my world. All that’s left now are my beloved folding cameras, with their tactile folds and whispers of history, and two SLRs I just can’t part with. They’re like old friends I can’t bear to lose, even if they sit gathering dust.
Looking back, I’ve been dancing with this shadow for longer than I care to admit. As a kid, doctors warned I’d lose my sight in adolescence. It didn’t happen, praise God for that grace, and maybe that’s why I’ve poured everything into photography. Forty years as a hobbyist, twenty as a professional. Every click was a prayer, a moment stolen from time.
Through breakups and breakthroughs, lean years and laughter, that passion kept me steady. It wasn’t about fame or perfection; it was joy, pure and simple. Losing it? It’s like misplacing a limb. For months, I’ve wandered aimlessly, future a foggy outline. But I’m not alone in the drift, Jesus has been my anchor, my wife my soft place to land, and our three goofy pups? They’re the daily reminder that wagging tails don’t need perfect vision.
Yesterday morning, something shifted. I woke with a spark, not a wildfire, just a gentle glow. Determination, I suppose you’d call it. I dug into a folder of unreleased shots from a May trip, landscapes that still make my heart hum even if I can’t see them sharply anymore. I posted a few, tentative steps back into sharing. I didn’t head out to shoot, but the thought lingered, whispering maybe. The truth is, I hold myself to impossible standards, flawless light, impeccable lines that I wouldn’t dream of expecting from anyone else. It’s a humble brag wrapped in humility: I’ve been blessed with skill, but pride can be a sneaky thief. How do I create without chasing ghosts of what was?
This road to blindness? I wouldn’t wish it on my worst enemy. It’s lonely, riddled with “what ifs” that echo in the quiet hours. But here’s the quiet miracle: it led me to the blind center in Phoenix. Walking through those doors flipped the script. Suddenly, it wasn’t the end of my story but a pivot to a new chapter. I’ve met folks who get it, the raw grief, the stubborn spark. Some love photography as fiercely as I do, swapping tips on adaptive gear like it’s the most natural conversation. Together, we’ve sparked an advocacy group here in Arizona, a loose band of encouragers lifting each other up. No heroes among us, just people saying, “Hey, you’ve got this—one step at a time.”
Life’s gone tactile now, and there’s a strange beauty in that. Braille bumps under my fingers, keyboard clicks like Morse code for my thoughts. Cameras with dials and buttons? They’re gold, things I can map in my mind, muscle memory overriding the dark. Tomorrow, I’m pulling out my Minolta Maxxum, that autofocus wonder with its forgiving heart. I’ll give it a go, no pressure, just curiosity.
Scanning the negatives afterward will be a puzzle, details lost to me, but that’s the thrill, isn’t it? An adventure in trust, handing the reveal over to the machine and whatever magic it uncovers.
I love this part, if I’m honest, the relearning. Figuring out angles by sound and feel, composing by instinct honed over lifetimes. Lights? Who needs ’em? I navigate just fine in the pitch black, a skill that’s equal parts survival and secret superpower. It’s all a gift, wrapped in loss, reminding me that sight was never the whole picture.
If you’re reading this and facing your own storm—big or small—know this: it’s okay to sit on that bench for a while. But don’t stay there forever. Reach for the hand extended, whether it’s a friend’s, a stranger’s at a support group, or the steady one from above. I’m still figuring it out, one humble frame at a time. Life? It’s good. Messy, blurred at the edges, but profoundly good.
Thanks for letting me share. Drop a note if this resonates. I’m all ears (and heart). Until next time, keep chasing what lights you up, however dim the path.
With quiet thanks,
Jefferson Davis

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Diamondbacks OneCourt
Last Sunday, my wonderful wife, Deana, and I headed to Chase Field in Phoenix for an exciting Arizona Diamondbacks game against the Boston Red Sox. As a newly blind baseball fan, I’ve always loved the energy of live games, but navigating the sensory overload of a stadium can be daunting. Thankfully, Deana, being the incredible wife that she is, had planned ahead and reserved a One Court device for me to use during the game. This innovative technology, designed specifically for blind and visually impaired fans, has been a game changer.
The Arizona Diamondbacks hold the distinction of being the first MLB team to offer One Court devices, a remarkable step toward inclusivity. These devices are tailored to help blind and visually impaired fans follow the game through audio play-by-play announcements and tactile feedback. Chase Field keeps ten of these devices charged and ready for use, available upon request at no extra cost. Knowing this, Deana had called ahead to ensure one was reserved for me, making our trip to the ballpark even more special.
For those unfamiliar, the One Court device is a compact, lap gadget that delivers real-time game updates. It vibrates to indicate action on specific bases and provides audible commentary through earpieces, allowing users to track the game’s flow. It’s not perfect, but it’s a fantastic tool that bridges the gap for visually impaired fans, letting us feel closer to the action.
Walking into Chase Field is always a whirlwind. The buzz of the crowd, the echo of announcements, and the chatter of vendors create a chaotic symphony that can be disorienting for someone who is blind or visually impaired. I’ve been to the stadium before, but the energy still feels overwhelming at times. Fortunately, the staff at Chase Field are exceptional. From the moment we arrived, someone was there to guide us, ensuring we felt comfortable and supported.
Deana handled the paperwork to check out the One Court device. Once that was sorted, we made our way to our ADA-accessible seats. These seats are a blessing, offering plenty of space so I didn’t have to worry about accidentally bumping anyone with my cane. The stadium staff even stopped by to check in, making sure I understood how to use the device and answering any questions. Their attentiveness set the tone for a fantastic day.
As the game began, the One Court device sprang into action. It provided play-by-play updates, describing each pitch, hit, and fielding play with detail. The tactile feedback was particularly cool, different vibrations corresponded to action at specific bases, helping me visualize where the runners were. It felt like I was right in the middle of the game, calling plays like a sports broadcaster.
There was a slight hiccup, though. My hearing aids made it tricky to hear the audio clearly through the device’s earpieces. The stadium noise didn’t help either! I mentioned this to the staff, and they suggested trying a different set of earpieces next time, which I’ll definitely do. Despite the audio challenge, the device still allowed me to follow the game closely, and I was grateful for the experience it provided.
The Diamondbacks and Red Sox were locked in a tight battle, staying tied through the first six innings. I kept up with the plays through the One Court device, but I found myself turning to Deana to ask for the score. Little did I know, the device has an “Info” button that provides score updates on demand! I felt a bit silly when I learned this afterward, but it’s something I’ll remember for next time.
In the seventh inning, the Red Sox pulled ahead, scoring three runs in a classic late-inning surge they’re known for. Despite a pitching change, the D-Backs couldn’t recover, and Boston clinched the win. It was a tough loss, but the excitement of the game and the vibrant atmosphere at Chase Field made it an unforgettable day. Deana and I cheered, laughed, and soaked in the experience, loss and all.
The One Court device truly enhanced my experience at Chase Field. Being able to follow the game’s action through audio and tactile feedback made me feel more connected to the sport I love. Aside from the audio issue with my hearing aids, I wished the device automatically announced the score periodically. Adding a Braille display for score updates would be a dream, though I understand that could be costly. Still, the device is a huge step forward, and I’m excited to see how future versions might improve.
For any blind or visually impaired baseball fans, I wholeheartedly recommend giving the One Court device a try. It’s free to use, and the Diamondbacks’ staff make the process easy. The device doesn’t just let you follow the game; it empowers you to engage with it in a way that feels immersive and inclusive. I felt like I was part of the action, calling out plays and cheering alongside everyone else.
Our day at Chase Field was about more than just baseball, it was about shared moments, accessibility, and the joy of being part of the crowd. Deana’s thoughtfulness in reserving the One Court device and the stadium staff’s dedication to ensuring we had a great time made the experience truly special. We left the ballpark with big smiles, already looking forward to our next game.
If you’re a blind or visually impaired fan considering a trip to Chase Field, don’t hesitate to request a One Court device. It’s a fantastic tool that brings the game to life in ways I hadn’t imagined.
Have you tried the One Court?
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Blob City
I’ve spent many sleepless nights trying to find the right words to describe what it’s like to go completely blind. It’s not like flipping off a light switch! For most people who are blind, about 90% according to the stats, there’s still something to see. Maybe it’s just light perception, like knowing the sun’s out there doing its thing, or maybe it’s catching a glimpse of colors, like a fuzzy rainbow. But for a few folks I know who’ve been completely blind since birth, sight is just one piece of the sensory puzzle, and they prove you can live a full, vibrant life without it. Me? I’m somewhere near the end, navigating a world of blobs, and let me tell you, it’s a wild ride.
Let’s get one thing straight: life without sight isn’t easy, but it’s absolutely worth living to the fullest. I mean, who needs 20/20 vision when you’ve got stubbornness, a good sense of humor, and a knack for dodging furniture? (I still bump into things, but I’m working on my ninja skills.) The world of blindness is filled with challenges, but it’s also brimming with possibilities. I love chatting with people about the tech that’s out there, like screen readers, smart canes, apps that describe the world like a chatty tour guide. But the real MVP in my life is Braille.
Braille is like the secret handshake of the blind community. It’s tactile, it’s elegant, and it keeps my brain as sharp as a tack. Fun fact: reading braille lights up the same part of your brain as reading with your eyes. So, while I’m running my fingers over those delightful dots, I’m basically doing mental push-ups. Without braille, I’m not sure I’d be as happy as I am today. It’s my bridge to a world of books, notes, and magazines.
I’ve been blind in one eye since I was a day old, thanks to a condition called Septo-Optic Dysplasia, which led to Optic Atrophy. Sounds like a villain from a sci-fi flick, right? Basically, it means my optic nerve cells are slowly checking out, like guests leaving a party early. Back in the 1970s, though, I didn’t let that stop me. I was just another kid, tearing around on bikes and motorcycles, channeling my inner Evel Knievel. Sure, I had more crashes than the average daredevil—my nickname was and still is “Crash”—but I didn’t care. My parents were my biggest cheerleaders, telling me I could do anything. I still believe them.
In January 2024, my doctor dropped a bombshell: “Stop driving.” The next month, another gut-punch: I had about two years of sight left. We hoped it’d stretch longer, but my vision had other plans. Right now, I’m down to five degrees of peripheral vision, and it’s blurry, like looking through a foggy window. Everyone and everything is a blob. My wife, Deana has been my rock through this whole journey, encouraging me to keep going, even when I’m tempted to throw a pity party for one.
Here’s what it’s like to live in Blob City. I can still pick up colors, so I might notice a red hat or a green shirt, but details? Forget it. Reading text is like trying to solve a puzzle in a windstorm. I have to stare at it forever, and it better be in font size “Billboard.” Walking, though, is my jam. It clears my head and usually puts me in a better mood. This morning, I strolled down to Green Valley Park, looped around the lake, and decided to grab Deana a drink from the gas station on the way back. Easy, right? Wrong.
I sauntered up to the cooler, ready to be the hero of hydration, only to remember I couldn’t read the labels. Picture me, squinting like a detective at a crime scene, trying to guess which bottle was Deana’s favorite. I grabbed one that looked vaguely familiar and hoped for the best. Then, a kind stranger piped up: “Need any help?” I could’ve hugged him. He confirmed I’d picked the right drink, then asked, “How’d you figure that out?” I explained my blob-vision situation, and he was surprised. Like most folks, he saw my white cane and dark glasses and assumed I was living in total darkness. Nope, just blob central.
That white cane and dark glasses? It’s like the unofficial “blind uniform.” People see it and assume I can’t see a thing, which is honestly a safe bet. I don’t mind the assumptions, better safe than sorry, right? Most people are just trying to help, and I’m grateful for it. I always say “thank you,” even if I don’t need the assistance. The other day, someone offered to guide me across the street, and I thought, Buddy, I’ve been crossing streets since disco was king. But I smiled, said thanks, and let them feel like a superhero. It’s a win-win.
The truth is, every blind person’s experience is different. Some of us see blobs, some see light, some see nothing at all. What we all share is the ability to adapt, to find joy in the little things, and to keep moving forward. For me, that means laughing at my own misadventures, like the multiple times I called a Mister a Misses or vice versa. That can get dicey really quick.
Losing my sight hasn’t been easy, but it’s taught me to lean into life’s unpredictability. I’m still the kid who rode motorcycles and dreamed big, just with a few more battle scars and a better sense of humor. With Deana by my side, braille to keep me sharp, and the occasional kind stranger to point me toward the right soda, I’m living a life that’s full, messy, and mine. So here’s to the blobs. May they always be colorful, and may I never stop finding the humor in this wild, blurry world.
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f/128 Intro
In this short introduction episode of f/128, I discuss why I’m doing this podcast and how I can help others navigate the challenges and joys of life. Drawing from my personal experience, I also share the adventure of going blind and how it reshaped my relationship with the world, particularly as a passionate lover of film photography. The journey will be transformative, revealing unexpected beauty and creativity in each moment. I believe the insights and stories I share can inspire and empower others who might be facing their own obstacles. Together, we will explore the nuances of photography, discuss techniques, and delve into the stories behind the images that capture our experiences. Please join me on this fantastic adventure of a lifetime, where we celebrate not only the art of photography but also resilience and the human spirit in the face of adversity.

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Stuck
As I pen this entry, I hope it will mark the end of a series of “blind” updates for some time. Have you ever found yourself in an inescapable predicament? My dialogue will carefully omit any direct reference to my employer, a vast global entity. Before the devastating prognosis of my impending blindness, and the ensuing revocation of my driving privileges, I found fulfillment in my profession and thrived on a perfect work routine.
My earlier schedule had me traveling to a neighboring town for work, beginning at 5:00 AM and ending at 1:30 PM from Monday to Friday. My return home was typically around 2:00 PM, allowing me the luxury of a brief rest before tending to household duties and at times, preparing dinner for my wife, Deana. This routine suited us well, allowing us to enjoy our evenings together, and even catch a movie after her workday had concluded.
Following the dire revelation about my vision, I was compelled to request a transfer to a branch within walking proximity to my home. This transition was protracted, lasting a month, with three weeks in which I received no compensation. My role in the corporation pertained to merchandising—a field I had not sought academic training for nor anticipated finding enjoyable. However, my penchant for order, structure, and meticulous tasks seemed to align well with the demands of the role.
Despite my capability and experience to perform my job without sight, the company reassigned me to an in-store position, with working hours slated from 1:30 PM to 10:00 PM on arbitrary days. My wife’s schedule has her leaving for work at 8:00 AM, during which I stay with our dogs until she returns at lunch to drive me to work. Consequently, we have been deprived of the cherished evenings we once shared. My new role demands squinting at minute details, which results in intense eye strain and headaches by day’s end.
While my employer has fulfilled the legal obligations, their support has not extended beyond that. My objections to this decision are manifold. I am naturally inclined towards early mornings, valuing the ability to complete my workday ahead of time and spend evenings with my loved ones.
Pursuing alternative employment remains a viable option, yet I am faced with the dilemma that full disclosure of my visual impairment may render me unemployable. While part-time work is attainable, it would compromise my access to quality health insurance. The coverage I currently hold is excellent, but parting ways with my job or reducing hours would precipitate a twofold increase in insurance costs. My wife’s insurance plan does not cover dependents, which further immobilizes me in my current role.
My aspirations for financial support through my blog and magazine, alongside print sales, have yet to yield significant results, though I express my deepest gratitude to everyone who has engaged with my work.
Under South Carolina’s regulations, disability benefits are inaccessible to me until my vision constricts to 20 degrees or less; currently, it stands at approximately 40 degrees. The Commission for the Blind is a resource, but its primary focus is to ensure employment for the visually impaired. Despite these challenges, I am determined to persevere in the hope of a breakthrough, but the everyday struggle is real, with a mortgage and other bills aligning with the fiscal responsibilities that many of us face.
It is not my intent to lament my circumstances; however, I cannot ignore the reality of the corner I seem to be trapped in. I am contending with Septo Optic Dysplasia and Optic Atrophy, amongst a long list of other challenges, and yet I take solace in the fact that I’m still able to provide for my family—this is undeniably a positive. The unwavering support from my wife, Deana, has been nothing short of heroic, and her strength is a blessing for which I am eternally grateful.
Should anyone have practical suggestions for additional sources of income, I would be keen to hear them. We seek your ideas and assistance. While I seldom mention it, there is a tip jar situated on the right side of the blog—for those inclined to support my endeavors with the equivalent of a coffee, it would be greatly appreciated. In my forthcoming post, which you can expect on Monday, I will discuss my preferred and reasonably priced folding medium format camera.
While I have pursued photography as a business venture for several years, it has not been financially lucrative for me. The ordeal nearly overwhelmed me at times. Nevertheless, it is an endeavor that brings tranquility to my spirit. Its absence would leave a void within me — for it is intricately tied to my identity.
I am the individual who approaches others with enthusiasm about cameras, only to reveal that I am progressing towards blindness. This revelation often elicits surprise and confusion; however, I find a certain satisfaction in such reactions. People are strange, but so am I.
It is my intention to share my narrative with you, one that intertwines simplicity with complexity. I invite you to subscribe to this blog for further insights and to explore more of my photographic journey.









